Canonical Allele Identifier: CA2086412
Gene: CPS1 HGNC NCBI

Linked Data

dbSNP Id: rs121912592

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.210600636C>A , CM000664.2:g.210600636C>A GRCh38
NC_000002.11:g.211465360C>A , CM000664.1:g.211465360C>A GRCh37
NC_000002.10:g.211173605C>A NCBI36
NG_008285.1:g.127952C>A , LRG_336:g.127952C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000233072.10:c.1631C>A MANE Select ENSP00000233072.5:p.Thr544Lys
ENST00000430249.7:c.1649C>A ENSP00000402608.2:p.Thr550Lys
ENST00000451903.3:c.278C>A ENSP00000406136.2:p.Thr93Lys
ENST00000673510.1:c.1631C>A ENSP00000500537.1:p.Thr544Lys
ENST00000673630.1:c.1631C>A ENSP00000501073.1:p.Thr544Lys
ENST00000673698.1:c.111C>A
ENST00000673711.1:c.1631C>A ENSP00000501022.1:p.Thr544Lys
ENST00000674074.1:n.776C>A
ENST00000233072.9:c.1631C>A ENSP00000233072.5:p.Thr544Lys
ENST00000430249.6:c.1649C>A ENSP00000402608.2:p.Thr550Lys
ENST00000451903.2:c.278C>A ENSP00000406136.2:p.Thr93Lys
NM_001122633.2:c.1649C>A NP_001116105.1:p.Thr550Lys
NM_001122634.3:c.278C>A NP_001116106.1:p.Thr93Lys
NM_001875.4:c.1631C>A , LRG_336t1:c.1631C>A NP_001866.2:p.Thr544Lys
XM_011510640.1:c.1664C>A XP_011508942.1:p.Thr555Lys
XM_011510641.1:c.1631C>A XP_011508943.1:p.Thr544Lys
XM_011510642.1:c.1631C>A XP_011508944.1:p.Thr544Lys
XM_011510643.1:c.1631C>A XP_011508945.1:p.Thr544Lys
XM_011510644.1:c.1631C>A XP_011508946.1:p.Thr544Lys
NM_001122633.3:c.1631C>A NP_001116105.2:p.Thr544Lys
NM_001369256.1:c.1664C>A NP_001356185.1:p.Thr555Lys
NM_001369257.1:c.1631C>A NP_001356186.1:p.Thr544Lys
NM_001875.5:c.1631C>A MANE Select NP_001866.2:p.Thr544Lys
NR_161225.1:n.2540C>A
NR_163592.1:n.787C>A